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The official documents governing mental health services provision include arrangements providing for the rights of access to services, informed consent, the legal procedures in cases of statutory commitment, access to personal files, etc.
In special populations – those with low levels of literacy, different cultural traditions, a context of inequities, or where there is lack of health services, – informed consent requires special consideration.
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Furthermore, Gruskin et al. [ 49] and King et al. [ 50] advocates for consideration of the health and human rights of pregnant women when providing HIV testing services by observing informed consent procedures, maintenance of privacy and confidentiality [ 51].
Participants were provided with written study information by a lead stroke clinician within each service, and written informed consent was obtained at the start of each group interview.
Health service managers signed voluntary informed consent and were assured that the results for their site would not be identifiable in any reports and that the assessment would have no effect on them from the government program.
This study was reviewed and approved by an IRB (Ethical and Independent Review Services), all participants provided written informed consent prior to the focus group discussion session, and patient confidentiality and good research practices were followed throughout the course of the study.
Procedures were in accordance with NHS national research ethics service approval (10/H0707/29), and written informed consent was obtained.
Recruitment was carried through the Oxford Centre for Enablement and Opcare in accordance with NHS national research ethics service approval (10/H0707/29), and written informed consent was obtained.
If service users lack capacity to give informed consent to participate in a face to face interview, information about their activities in the preceding week is gathered from the case records and discussions with their primary nurse.
The study was reviewed and approved by Ethical and Independent Review Services IRB, all participants provided written informed consent prior to the interviews, and patient confidentiality and good research practices were followed throughout the course of the study.
In order to make the procedure more convenient, data collection would need to be regarded as a standard component of medical service [ 36], so that written informed consent would not be required for each assessment.
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